Tenofovir disoproxil fumarate is a prescription antiviral tablet. Its active ingredient is Tenofovir disoproxil fumarate, also called tenofovir DF or TDF. It belongs to a group of HIV medicines called nucleotide reverse transcriptase inhibitors. It is used to treat two long-term viral infections: HIV-1, where it is always taken together with other HIV medicines, and chronic hepatitis B, a long-term infection of the liver. Tenofovir-containing medicines are also prescribed to prevent HIV in people at high risk, an approach called pre-exposure prophylaxis, or PrEP. It lowers the amount of virus in the body but does not remove the virus, so treatment is usually long term.
Tenofovir disoproxil fumarate is a tablet taken by mouth once a day. The body changes the medicine into its active form, tenofovir, inside the cells. Tenofovir blocks two viral enzymes: reverse transcriptase, which HIV uses to copy itself, and the hepatitis B polymerase, which the hepatitis B virus needs to copy its DNA. With these enzymes blocked, the viruses cannot multiply as fast, so the amount of virus in the blood falls.
In HIV care, Tenofovir disoproxil fumarate is one part of a combination of medicines. It is never used on its own for HIV, because the virus quickly becomes resistant when a single medicine is used alone. In chronic hepatitis B, the World Health Organization recommends tenofovir as a preferred first-line antiviral, because it works well and resistance to it develops slowly. Hepatitis B treatment is usually long term, and many people continue it for years.
The medicine comes as 300 mg tablets, which contain the same amount of active ingredient as the 245 mg tablets sold in the European Union. Lower-strength tablets and an oral powder are made for children. It can be taken with or without food.
Tenofovir disoproxil fumarate needs medical supervision. The US label carries two boxed warnings, the strongest type of warning a medicine can have. The first is a rare but serious build-up of acid in the blood called lactic acidosis, together with an enlarged, fatty liver. The second is a flare of hepatitis B that can happen when treatment is stopped. The medicine can also harm the kidneys and lower bone mineral density, so kidney and liver blood tests are done before treatment starts and during treatment. Tell your doctor about every other medicine you take, especially painkillers such as ibuprofen and naproxen, because some medicines add to the strain on the kidneys. Do not stop this medicine on your own.
Tenofovir disoproxil fumarate is used for:
Common Side Effects (Usually Mild and may lessen with continued use)
Serious Side Effects (Seek Urgent Medical Attention)
Tenofovir disoproxil fumarate is a prodrug. A prodrug is a medicine that is not active when it is swallowed; the body has to change it into the active form. Here, the body strips away part of the molecule and leaves tenofovir, which then has two phosphate groups added inside the cells. The finished product is called tenofovir diphosphate, and this is the form that fights the viruses.
Tenofovir diphosphate is an acyclic nucleoside phosphonate. In plain words, it is a small, flexible molecule built to look like adenosine, one of the four building blocks that viruses use to copy their genetic material. When HIV reverse transcriptase or the hepatitis B polymerase tries to copy the virus and picks up tenofovir diphosphate by mistake, the new chain of DNA cannot grow any further. This is known as chain termination.
Reverse transcriptase is the enzyme HIV uses to turn its RNA into DNA, a step it must complete before it can settle into a human cell. The hepatitis B polymerase does a similar job for the hepatitis B virus. Blocking these enzymes slows both viruses down, which is why the amount of virus in the blood falls and why the immune system gets a chance to recover.
Because the target is a viral enzyme and not a human one, the medicine does not kill cells directly. It also stays inside cells for a long time, so one tablet a day keeps working around the clock.
The US label does not list Tenofovir disoproxil fumarate as harmful to an unborn baby, and it does not ask for contraception. Animal studies using high doses showed no harm to the developing baby, and studies in pregnant women have been too few to give a firm answer. The label asks doctors to report pregnancies to the Antiretroviral Pregnancy Registry. The World Health Organization recommends antiviral treatment in pregnancy for women with hepatitis B, to lower the chance of passing the virus to the baby. Tell your doctor if you are pregnant or planning a pregnancy, and do not stop treatment on your own.
Tenofovir passes into human milk. The label advises mothers with HIV not to breastfeed, because HIV can pass to the baby through breast milk and because of the risk of serious reactions in the baby. If you have hepatitis B and you are breastfeeding, talk to your doctor about what is right for you and your baby.
The prescribing information does not list alcohol as an interaction with Tenofovir disoproxil fumarate. Heavy drinking is hard on the liver, and hepatitis B already affects the liver, so keeping alcohol to a minimum is sensible.
Dizziness is a common side effect. If you feel dizzy, do not drive, cycle or use tools or machines until you feel well again.
Tenofovir disoproxil fumarate is cleared from the body by the kidneys. The label says kidney tests (creatinine clearance, phosphate, urine glucose and urine protein) should be checked before treatment and during it. Creatinine clearance is a blood test that shows how well your kidneys are filtering. If kidney function is reduced, the dose is given less often. People on dialysis need a different schedule. Rarely, the medicine can damage the kidney tubes, causing Fanconi syndrome or kidney failure. Avoid other medicines that can harm the kidneys, such as high doses of painkillers like ibuprofen and naproxen.
Liver disease does not change the amount of Tenofovir disoproxil fumarate in the body, and the label says no dose change is needed. Rarely, the medicine can cause a build-up of acid in the blood with an enlarged, fatty liver. If you have hepatitis B, stopping treatment can cause a serious flare, so liver blood tests are checked before treatment, during it, and for several months after it ends.
The US label describes use in children from 2 years of age for HIV-1, and from 12 years of age for chronic hepatitis B, with the 150 mg, 200 mg and 250 mg tablets or an oral powder for children who cannot swallow the adult tablet. In the European Union, treatment is authorised for chronic hepatitis B in children from 2 years of age who have compensated liver disease (liver disease where the liver is still working properly), using lower-strength tablets or granules.
The clinical trials did not include enough people aged 65 and over to show whether they respond differently from younger people. The label advises careful dose selection for older people, because kidney function is often reduced with age. Kidney function is usually checked before and during treatment.
Get medical help straight away if you have:
Therapeutic Class
Antiviral; antiretroviral (nucleotide reverse transcriptase inhibitor) for HIV-1 infection and chronic hepatitis B
Action Class
Nucleotide reverse transcriptase inhibitor; blocks HIV-1 reverse transcriptase and hepatitis B virus polymerase
Chemical Class
Acyclic nucleoside phosphonate diester; fumaric acid salt and prodrug of tenofovir
Habit Forming
No
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